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Clinical Trial Summary

It is a prospective cohort study.The primiparas in six geographic regions of China are recruited to observe the natural recovery of pelvic floor muscle. The pelvic floor muscle function is evaluated at 6 weeks,3 months and 12 months after delivery.


Clinical Trial Description

The primiparas in six geographic regions of China are recruited to observe the natural recovery of pelvic floor muscle.Evaluation of pelvic floor function is performed at 6 weeks, 3 months, 12 months after delivery. The modified Oxford Grading Scale and Levator ani testing are used to quantify PFM strength through vaginal palpation. Pelvic floor muscles strength, endurance, repetition,vaginal contraction pressure and the knack test are evaluated using a neuromuscular stimulation therapy system of PHENIX (Company: Vivaltis -Electronic Concept Lignon Innovation, Montpellier, France). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03506204
Study type Observational [Patient Registry]
Source Peking Union Medical College Hospital
Contact Zhijing Sun, MD
Phone 13651314354
Email sunzhj2001@sina.com
Status Recruiting
Phase
Start date May 10, 2018
Completion date December 31, 2020

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